Publications by authors named "Matteo M Guerrini"

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Cap analysis of gene expression (CAGE) and noncoding regulatory elements.
Matteo Maurizio Guerrini, Akiko Oguchi, Akari Suzuki, Yasuhiro Murakawa

Semin Immunopathol· January 2022

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Functional genetics for studying the human immune system.
Kazuhiko Yamamoto, Akari Suzuki, Matteo Maurizio Guerrini

Int Immunol· November 2021

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Functional genomics of autoimmune diseases.
Akari Suzuki, Matteo Maurizio Guerrini, Kazuhiko Yamamoto

Ann Rheum Dis· June 2021

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Detection of a High-Turnover Serotonin Circuit in the Mouse Brain Using Mass Spectrometry Imaging.
Eiji Sugiyama, Matteo M Guerrini, Kurara Honda, Yuko Hattori, Manabu Abe

iScience· October 2019

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Microbiota - an amplifier of autoimmunity.
Alexis Vogelzang, Matteo M Guerrini, Nagahiro Minato, Sidonia Fagarasan

Curr Opin Immunol· December 2018

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A Hen in the Wolf Den: A Pathobiont Tale.
Matteo M Guerrini, Alexis Vogelzang, Sidonia Fagarasan

Immunity· April 2018

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Metabolic shift induced by systemic activation of T cells in PD-1-deficient mice perturbs brain monoamines and emotional behavior.
Michio Miyajima, Baihao Zhang, Yuki Sugiura, Kazuhiro Sonomura, Matteo M Guerrini

Nat Immunol· December 2017

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RANKL expressed on synovial fibroblasts is primarily responsible for bone erosions during joint inflammation.
Lynett Danks, Noriko Komatsu, Matteo M Guerrini, Shinichiro Sawa, Marietta Armaka

Ann Rheum Dis· June 2016

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Inhibition of the TNF Family Cytokine RANKL Prevents Autoimmune Inflammation in the Central Nervous System.
Matteo M Guerrini, Kazuo Okamoto, Noriko Komatsu, Shinichiro Sawa, Lynett Danks

Immunity· December 2015

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The immune system, bone and RANKL.
Matteo M Guerrini, Hiroshi Takayanagi

Arch Biochem Biophys· November 2014

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Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO.
Nadia Lo Iacono, Harry C Blair, Pietro L Poliani, Veronica Marrella, Francesca Ficara, Matteo M Guerrini

J Bone Miner Res· December 2012

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RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations.
Alessandra Pangrazio, Barbara Cassani, Matteo M Guerrini, Julie C Crockett, Veronica Marrella

J Bone Miner Res· February 2012

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Infantile malignant, autosomal recessive osteopetrosis: the rich and the poor.
Anna Villa, Matteo M Guerrini, Barbara Cassani, Alessandra Pangrazio, Cristina Sobacchi

Calcif Tissue Int· January 2009

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Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations.
Matteo M Guerrini, Cristina Sobacchi, Barbara Cassani, Mario Abinun, Sara S Kilic

Am J Hum Genet· July 2008

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Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.
Cristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, Mario Abinun, Alessandra Pangrazio

Nat Genet· August 2007

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Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)-deficient mice and corrects their immune and metabolic defects.
Alessandra Mortellaro, Raisa Jofra Hernandez, Matteo M Guerrini, Filippo Carlucci, Antonella Tabucchi

Blood· November 2006

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